2-thiaspiro[3.5]nonan-7-one

97%

Reagent Code: #238635
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CAS Number 1557247-28-5

science Other reagents with same CAS 1557247-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.2453 g/mol
Formula C₈H₁₂OS
badge Registry Numbers
MDL Number MFCD30002863
thermostat Physical Properties
Boiling Point 285.9±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a building block in organic synthesis, especially in the development of pharmaceuticals and bioactive molecules. Its unique spirocyclic structure containing a sulfur atom enhances stability and influences molecular conformation, making it valuable in drug design for exploring new chemical space. It is also employed in the synthesis of specialty heterocyclic compounds where ring strain and polarity play a role in reactivity. Due to its ketone functionality, it participates in nucleophilic addition and condensation reactions, enabling further functionalization for use in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,040.00
inventory 250mg
10-20 days ฿8,070.00
2-thiaspiro[3.5]nonan-7-one
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Used primarily as a building block in organic synthesis, especially in the development of pharmaceuticals and bioactive molecules. Its unique spirocyclic structure containing a sulfur atom enhances stability and influences molecular conformation, making it valuable in drug design for exploring new chemical space. It is also employed in the synthesis of specialty heterocyclic compounds where ring strain and polarity play a role in reactivity. Due to its ketone functionality, it participates in nucleophili

Used primarily as a building block in organic synthesis, especially in the development of pharmaceuticals and bioactive molecules. Its unique spirocyclic structure containing a sulfur atom enhances stability and influences molecular conformation, making it valuable in drug design for exploring new chemical space. It is also employed in the synthesis of specialty heterocyclic compounds where ring strain and polarity play a role in reactivity. Due to its ketone functionality, it participates in nucleophilic addition and condensation reactions, enabling further functionalization for use in medicinal chemistry research.

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